drugset / Trial / NCT05030415
Ixekizumab in Adult Patients With Lichen Planus and Lichen Planopilaris
NaSingle-groupOpen-labelTreatment
Summary
To evaluate the safety and efficacy of ixekizumab in lichen planus and lichen planopilaris clinical response by Total Body Surface (TBS) determination, Investigator Global Assessment (IGA) Score, Lichen Planopilaris Activity Index (LPPAI), and Frontal Fibrosing Alopecia Severity Score (FFASS).
Timeline
- Start
- 2021-08-12
- Primary completion
- 2024-03-25
- Completion
- 2024-03-25
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Ixekizumab | Monoclonal antibody | 80 mg | Subcutaneous |